chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	96131999	96132000	A	C	8	GENIC	homozygous	118051571
10	96136559	96136560	A	G	15	GENIC	possibly homozygous	116689367
10	96136661	96136662	A	G	30	GENIC	possibly homozygous	116689375
10	96143050	96143051	A	T	5	GENIC	homozygous	118009790
10	96143056	96143057	G	T	4	GENIC	homozygous	118009791
10	96143064	96143065	G	T	3	GENIC	homozygous	118009792
10	96143154	96143155	G	T	2	GENIC	homozygous	118009793
10	96143166	96143167	C	T	14	GENIC	homozygous	118009794
10	96146524	96146525	A	T	44	GENIC	heterozygous	118085901
10	96158657	96158658	A	T	28	GENIC	heterozygous	118009795
10	96159656	96159657	A	T	31	GENIC	heterozygous	118051589
10	96162327	96162328	G	C	18	GENIC	homozygous	118051591
10	96163866	96163867	G	T	12	GENIC	homozygous	118051592
10	96164370	96164371	C	A	7	GENIC	heterozygous	118085902
10	96163870	96163871	C	T	12	GENIC	homozygous	118051594
10	96163871	96163872	A	G	12	GENIC	homozygous	118051596